Playtex 00220Recalls & reported problems
Edgewell Personal Care Brands, LLC · Playtex Sport 32ct MultiPk Odorshield Scented · Class 2
All models of Playtex (9)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00078300002208), received between Jul 28, 2016 and Jul 28, 2016 — classified as 1 injury.
The most frequently reported specific device problem is “Patient-Device Incompatibility” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Patient-Device Incompatibility1
Patient problems
- Toxic Shock Syndrome1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 28, 2016Patient-Device Incompatibility; Patient-Device Incompatibility
CONSUMER REPORTED THAT WITHIN AN HOUR OF USING THE PRODUCT SHE DEVELOPED A HIGH FEVER, VOMITING AND DIARRHEA, BUT SYMPTOMS SUBSIDED UPON REMOVAL OF THE PRODUCT. SHE SOUGHT MEDICAL ATTENTION TWO DAYS LATER BUT NO TREATMENT WAS PRESCRIBED. CONSUMER REPORTS THAT "HER DOCTOR STATED HER SYMPTOMS WERE MORE THAN LIKELY TSS." CONSUMER ADDED SHE HAD SYMPTOMS OF TSS A FEW YEARS AGO BUT DID NOT SEEK MEDICAL ATTENTION AT THAT TIME.
Patient problems: Toxic Shock Syndrome
MAUDE report 5831544 ↗
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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